Genome-wide Mapping of Off-Target Events in Single-Stranded Oligodeoxynucleotide-Mediated Gene Repair Experiments: Molecular Therapy

Expanding the Potential of Mammalian Genome Engineering via Targeted DNA Integration

Frontiers Tissue Specific DNA Repair Outcomes Shape the Landscape of Genome Editing

Precise CRISPR-Cas–mediated gene repair with minimal off-target and unintended on-target mutations in human hematopoietic stem cells

Full article: CRISPR/Cas9 (D10A) nickase-mediated Hb CS gene editing and genetically modified fibroblast identification

Massively targeted evaluation of therapeutic CRISPR off-targets in cells

MDM2 antagonists promote CRISPR/Cas9-mediated precise genome editing in sheep primary cells: Molecular Therapy - Nucleic Acids

Cells, Free Full-Text

Applications of genome editing technology in the targeted therapy of human diseases: mechanisms, advances and prospects

Progress and harmonization of gene editing to treat human diseases: Proceeding of COST Action CA21113 GenE-HumDi: Molecular Therapy - Nucleic Acids

Targeting double-strand break indel byproducts with secondary guide RNAs improves Cas9 HDR-mediated genome editing efficiencies

Increasing CRISPR Efficiency and Measuring Its Specificity in HSPCs Using a Clinically Relevant System: Molecular Therapy - Methods & Clinical Development